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2,4,6(1H,3H,5H)-Pyrimidinetrione, 1-cyclohexyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1015-65-2

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1015-65-2 Usage

Physical form

White crystalline solid

Odor

Faint

Primary use

Stabilizer in plastics (e.g. PVC)

Function

Prevents degradation of plastic due to heat, UV light, and oxidation

Other uses

Flame retardant and industrial additive

Safety precautions

Handle with caution and follow safety guidelines

Check Digit Verification of cas no

The CAS Registry Mumber 1015-65-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,0,1 and 5 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1015-65:
(6*1)+(5*0)+(4*1)+(3*5)+(2*6)+(1*5)=42
42 % 10 = 2
So 1015-65-2 is a valid CAS Registry Number.

1015-65-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 10, 2017

Revision Date: Aug 10, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-cyclohexyl-1,3-diazinane-2,4,6-trione

1.2 Other means of identification

Product number -
Other names 1-cyclohexylpyrimidine-2,4,6(1H,3H,5H)-trione

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1015-65-2 SDS

1015-65-2Downstream Products

1015-65-2Relevant articles and documents

A facile synthesis of 5-acylbarbituric acids under microwave irradiations

Singh, Palwinder,Paul, Kamaldeep

, p. 1105 - 1108 (2007/10/03)

N-Monosubstituted and N,N'-disubstituted barbituric acids on treatment with benzoic anhydride/acetic anhydride under microwave irradiations without using any solvent provide a convenient methodology for the synthesis of 5-benzoyl/ acylbarbituric acids in moderate to high yields.

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